Abnormal DaTSCAN and Atypical Parkinsonism in SCA12
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DOI: 10.1002/mdc3.12751
Abstract: The spinocerebellar ataxias (SCAs) are a heterogeneous group of autosomal dominantly inherited progressive ataxia disorders, with a variable clinical presentation. More than 40 gene loci and mutations have been identified so far; however, an expansion… read more here.
Keywords: sca12; parkinsonism sca12; atypical parkinsonism; abnormal datscan ... See more keywords
Asymmetry of Tremor in Spinocerebellar Ataxia 12‐ Exception or Rule?
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DOI: 10.1002/mdc3.13237
Abstract: Spinocerebellar Ataxia 12(SCA12) is a rare form of SCA, predominantly reported in the ethnic Agarwal population originating from North India. It generally presents with late onset upper limb tremor followed by ataxia. Tremor in SCA12… read more here.
Keywords: spinocerebellar ataxia; exception; sca12; asymmetry ... See more keywords
PSP‐Like Phenotype in Genetically Confirmed SCA12
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DOI: 10.1002/mdc3.13590
Abstract: Spinocerebellar ataxia type 12 (SCA12) is an autosomal domi-nant cerebellar ataxia caused by CAG repeat expansions in the protein phosphatase 2 regulatory subunit B beta (PPP2R2B) gene in chromosome 5q. 1 The prevalence of SCA12… read more here.
Keywords: psp like; sca12; confirmed sca12; genetically confirmed ... See more keywords